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Characterization of pFMBL1, a small cryptic plasmid isolated from Leuconostoc mesenteroides SY2

Authors
Jeong, Seon-JuPark, Jae-YongLee, Hyong JooKim, Jeong Hwan
Issue Date
May-2007
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Leuconostoc mesenteroides; cloning vector; theta replication; Kimchi
Citation
PLASMID, v.57, no.3, pp 314 - 323
Pages
10
Indexed
SCIE
SCOPUS
Journal Title
PLASMID
Volume
57
Number
3
Start Page
314
End Page
323
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/28387
DOI
10.1016/j.plasmid.2006.09.003
ISSN
0147-619X
1095-9890
Abstract
A 4661 bp cryptic plasmid, pFMBL1, was isolated from Leuconostoc mesenteroides SY2, an isolate from Kimchi, and characterized. Nucleotide sequence analysis revealed two open reading frames, orf1 and orf2. orf2 was 453 bp in size and its translation product had 58% identity with a putative protein possibly involved in the replication of pTXL1, a cryptic plasmid from L. mesenteroides ssp. mesenteroides Y110. RNA transcript from orf2 was detected but not from orf1 or intergenic region. Minimum 3.5 kb fragment encompassing orf1 and orf2 was required for the replication of pFMBL1 and employed for the construction of Escherichia coli-Leuconostoc shuttle vector, pSJ33E. L. mesenteroides SY1 (another Kimchi isolate), Leuconostoc ssp., and Lactobacillus brevis were successfully transformed with pSJ33E, and the transformation efficiencies were ranged between 1.1 x 10(1) and 4 x 10(5) transformants/mu g DNA. No single-stranded DNA intermediate was detected from L. mesenteroides SY1 cells harboring pSJ33E, indicating that pFMBL1 probably replicated via theta-type mechanism. pSJ33E was stably maintained in L. mesenteroides SY1 in the absence of erythromycin (Em, 5 mu g/ml) and after 1 month of daily subculturing in MRS broth without selective pressure, three percent of cells still retained pSJ33E. (c) 2006 Elsevier Inc. All rights reserved.
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